Sulfur 8 Scalp Therapy Medicated Dandruff Control Scalp Butter Cream Ointment
FDA Label NDC 12022-035

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by J. Strickland And Co. for the product Sulfur 8 Scalp Therapy Medicated Dandruff Control Scalp Butter Cream (NDC 12022-035). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding drug facts, active ingredient, purpose, use, warnings, when using this product, stop use and consult a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient

Sulfur, 5%

Salicylic Acid, 3%

Purpose

Antidandruff

Use

  • relieves the itching and scaling associated with dandruff

Warnings

For external use only

When Using This Product

avoid contact with eyes. If contact occurs rinse eyes thoroughly with water.

Stop Use And Consult A Doctor If

  • condition worsens or does not improve after regular use as directed.
  • HAIR IS FLAMMABLE. Flammability is increased by product build-up. Keep hair away from sparks, flame, extreme heat or lit tobacco.

Keep Out Of Reach Of Children.

If swallowed, get medical help or call a Poison Control Center right away.

Directions

  • Apply a small amount to the scalp one to four times daily or as directed by a doctor.

Inactive Ingredients

Petrolatum, Mineral Oil, Tribehenin, Arachidyl Propionate, Polysorbate 20, Fragrance

* Please review the disclaimer below.